SnOct2-catalyzed and alcohol-initiated ROPs of L-lactide – About the influence of initiators on chemical reactions in the melt and the solid state

[Display omitted] •The established mechanism of SnOct2-catalyzed and alcohol-initiated ROPs of L-lactide needs modification.•The structure of the initiator has strong influence on transesterification in the melt and thus on the molecular weight distribution.•The end groups formed by the initiators a...

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Veröffentlicht in:European polymer journal 2021-06, Vol.153, p.110508, Article 110508
Hauptverfasser: Weidner, Steffen M., Meyer, Andreas, Falkenhagen, Jana, Kricheldorf, Hans R.
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Falkenhagen, Jana
Kricheldorf, Hans R.
description [Display omitted] •The established mechanism of SnOct2-catalyzed and alcohol-initiated ROPs of L-lactide needs modification.•The structure of the initiator has strong influence on transesterification in the melt and thus on the molecular weight distribution.•The end groups formed by the initiators also have an influence on transesterification reactions in the solid state.•These transesterification reactions involve the mobile and immobile amorphous phases, but not the interior of the crystallites. SnOct2 (Sn(II) 2-ethylhexanoate) catalyzed ROPs of L-lactide were performed in bulk with eight different alcohols as initiators. The time was varied between 1 h and 24 h for all initiators. For two initiators the temperature was also lowered to 115 °C. Even-numbered chains were predominantly formed in all polymerizations at short times, but the rate of transesterification (e.g. even/odd equilibration) and the molecular weight distribution were found to depend significantly on the nature of the initiator. Observed transesterification reactions also continued in solid poly(L-lactide), and with the most active initiator, almost total equilibration was achieved even at 130 °C. This means that all chains including those of the crystallites were involved in transesterification reactions proceeding across the flat surfaces of the crystallites. The more or less equilibrated crystalline polylactides were characterized by DSC and SAXS measurements with regard to their melting temperature (Tm), crystallinity and crystal thickness.
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SnOct2 (Sn(II) 2-ethylhexanoate) catalyzed ROPs of L-lactide were performed in bulk with eight different alcohols as initiators. The time was varied between 1 h and 24 h for all initiators. For two initiators the temperature was also lowered to 115 °C. Even-numbered chains were predominantly formed in all polymerizations at short times, but the rate of transesterification (e.g. even/odd equilibration) and the molecular weight distribution were found to depend significantly on the nature of the initiator. Observed transesterification reactions also continued in solid poly(L-lactide), and with the most active initiator, almost total equilibration was achieved even at 130 °C. This means that all chains including those of the crystallites were involved in transesterification reactions proceeding across the flat surfaces of the crystallites. 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SnOct2 (Sn(II) 2-ethylhexanoate) catalyzed ROPs of L-lactide were performed in bulk with eight different alcohols as initiators. The time was varied between 1 h and 24 h for all initiators. For two initiators the temperature was also lowered to 115 °C. Even-numbered chains were predominantly formed in all polymerizations at short times, but the rate of transesterification (e.g. even/odd equilibration) and the molecular weight distribution were found to depend significantly on the nature of the initiator. Observed transesterification reactions also continued in solid poly(L-lactide), and with the most active initiator, almost total equilibration was achieved even at 130 °C. This means that all chains including those of the crystallites were involved in transesterification reactions proceeding across the flat surfaces of the crystallites. The more or less equilibrated crystalline polylactides were characterized by DSC and SAXS measurements with regard to their melting temperature (Tm), crystallinity and crystal thickness.</description><subject>Alcohols</subject><subject>Balancing</subject><subject>Chemical reactions</subject><subject>Crystal structure</subject><subject>Crystallinity</subject><subject>Crystallites</subject><subject>Crystals</subject><subject>Flat surfaces</subject><subject>Initiators</subject><subject>L-lactide</subject><subject>MALDI-TOF</subject><subject>Melt temperature</subject><subject>Molecular weight distribution</subject><subject>Polylactic acid</subject><subject>Polymerization</subject><subject>Ring-opening polymerization</subject><subject>SAXS</subject><subject>Solid state physics</subject><subject>Tin(II) 2-ethylhexanoate</subject><subject>Transesterification</subject><issn>0014-3057</issn><issn>1873-1945</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNqFkc2KFDEUhYMo2I4-gwHX1d5UqlJVy2bwDxpaRl2HVHJDp0hX2iQltKt5B31Cn8TU9ODWRQi5nO8cbg4hrxlsGTDxdtriEs_BX07TtoaabRmDFvonZMP6jldsaNqnZAPAmopD2z0nL1KaAKDjgm_I7y_zQee60iorf_mJhqq5HK_DMfjKzS47lcv07vA50WDpvvJKZ2eQ_rn_RXdjWDLNR6Rutn7BWeMqesRCLMhM9RFPTitPI65omFMRPEAn9Pkhb32k4J2hKZe4l-SZVT7hq8f7hnx7_-7r7cdqf_jw6Xa3rzRveK5a09SsH8U4MmGUBcG5QdGjsEKIwQxqNLaGscG2Hwxoa4am1vXIxQhWq7bhN-TN1fccw_cFU5ZTWOJcImXdtiB6PnRdUXVXlY4hpYhWnqM7qXiRDORagZzkvwrkWoG8VlDI3ZXEssQPh1Em7dZPMi6iztIE91-Pvzvclx4</recordid><startdate>20210615</startdate><enddate>20210615</enddate><creator>Weidner, Steffen M.</creator><creator>Meyer, Andreas</creator><creator>Falkenhagen, Jana</creator><creator>Kricheldorf, Hans R.</creator><general>Elsevier Ltd</general><general>Elsevier BV</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8FD</scope><scope>JG9</scope></search><sort><creationdate>20210615</creationdate><title>SnOct2-catalyzed and alcohol-initiated ROPs of L-lactide – About the influence of initiators on chemical reactions in the melt and the solid state</title><author>Weidner, Steffen M. ; Meyer, Andreas ; Falkenhagen, Jana ; Kricheldorf, Hans R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c343t-5d4218b6bb16daf0633de68e6f6669d9abdf20b4e589d0cfd942c2b36b0fca543</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Alcohols</topic><topic>Balancing</topic><topic>Chemical reactions</topic><topic>Crystal structure</topic><topic>Crystallinity</topic><topic>Crystallites</topic><topic>Crystals</topic><topic>Flat surfaces</topic><topic>Initiators</topic><topic>L-lactide</topic><topic>MALDI-TOF</topic><topic>Melt temperature</topic><topic>Molecular weight distribution</topic><topic>Polylactic acid</topic><topic>Polymerization</topic><topic>Ring-opening polymerization</topic><topic>SAXS</topic><topic>Solid state physics</topic><topic>Tin(II) 2-ethylhexanoate</topic><topic>Transesterification</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Weidner, Steffen M.</creatorcontrib><creatorcontrib>Meyer, Andreas</creatorcontrib><creatorcontrib>Falkenhagen, Jana</creatorcontrib><creatorcontrib>Kricheldorf, Hans R.</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><jtitle>European polymer journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Weidner, Steffen M.</au><au>Meyer, Andreas</au><au>Falkenhagen, Jana</au><au>Kricheldorf, Hans R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>SnOct2-catalyzed and alcohol-initiated ROPs of L-lactide – About the influence of initiators on chemical reactions in the melt and the solid state</atitle><jtitle>European polymer journal</jtitle><date>2021-06-15</date><risdate>2021</risdate><volume>153</volume><spage>110508</spage><pages>110508-</pages><artnum>110508</artnum><issn>0014-3057</issn><eissn>1873-1945</eissn><abstract>[Display omitted] •The established mechanism of SnOct2-catalyzed and alcohol-initiated ROPs of L-lactide needs modification.•The structure of the initiator has strong influence on transesterification in the melt and thus on the molecular weight distribution.•The end groups formed by the initiators also have an influence on transesterification reactions in the solid state.•These transesterification reactions involve the mobile and immobile amorphous phases, but not the interior of the crystallites. SnOct2 (Sn(II) 2-ethylhexanoate) catalyzed ROPs of L-lactide were performed in bulk with eight different alcohols as initiators. The time was varied between 1 h and 24 h for all initiators. For two initiators the temperature was also lowered to 115 °C. Even-numbered chains were predominantly formed in all polymerizations at short times, but the rate of transesterification (e.g. even/odd equilibration) and the molecular weight distribution were found to depend significantly on the nature of the initiator. Observed transesterification reactions also continued in solid poly(L-lactide), and with the most active initiator, almost total equilibration was achieved even at 130 °C. This means that all chains including those of the crystallites were involved in transesterification reactions proceeding across the flat surfaces of the crystallites. The more or less equilibrated crystalline polylactides were characterized by DSC and SAXS measurements with regard to their melting temperature (Tm), crystallinity and crystal thickness.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><doi>10.1016/j.eurpolymj.2021.110508</doi></addata></record>
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subjects Alcohols
Balancing
Chemical reactions
Crystal structure
Crystallinity
Crystallites
Crystals
Flat surfaces
Initiators
L-lactide
MALDI-TOF
Melt temperature
Molecular weight distribution
Polylactic acid
Polymerization
Ring-opening polymerization
SAXS
Solid state physics
Tin(II) 2-ethylhexanoate
Transesterification
title SnOct2-catalyzed and alcohol-initiated ROPs of L-lactide – About the influence of initiators on chemical reactions in the melt and the solid state
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